Literature DB >> 15370545

A novel KERA mutation associated with autosomal recessive cornea plana.

Arif Khan1, Amr Al-Saif, Marios Kambouris.   

Abstract

PURPOSE: To report a novel KERA mutation associated with autosomal recessive cornea plana in members of a nuclear family and to describe their ophthalmic phenotypes.
METHODS: Ophthalmic examination, biometry, and direct sequencing of KERA.
RESULTS: Five of the 6 siblings were affected and had small flat corneas, variable anterior chamber depths, and short axial lengths. The remaining brother and the 2 parents had normal ophthalmic examinations. Genetic testing revealed a novel homozygous nonsense mutation in exon 3 [937C>T] in the clinically affected individuals. The clinically unaffected parents were confirmed as carriers. The clinically unaffected sibling had no KERA mutation. This mutation leads to replacement of an arginine by a stop codon at position 313 of keratocan protein.
CONCLUSIONS: This novel point mutation in KERA is the fourth thus far described. The ocular phenotype is characteristic of autosomal recessive cornea plana.

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Year:  2004        PMID: 15370545     DOI: 10.1080/13816810490514397

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  12 in total

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Authors:  Anthony J Aldave; George O D Rosenwasser; Vivek S Yellore; Jeanette C Papp; Eric M Sobel; Michele N Pham; Michael C Chen; Sugandha Dandekar; Ram Sripracha; Sylvia A Rayner; Joseph W Sassani; Michael B Gorin
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2.  Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation.

Authors:  A O Khan; M Aldahmesh; A Al-Saif; B Meyer
Journal:  Br J Ophthalmol       Date:  2005-11       Impact factor: 4.638

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5.  Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12.

Authors:  Michelle J Kim; Ricardo F Frausto; George O D Rosenwasser; Tina Bui; Derek J Le; Edwin M Stone; Anthony J Aldave
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Review 6.  Distribution and Function of Glycosaminoglycans and Proteoglycans in the Development, Homeostasis and Pathology of the Ocular Surface.

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Journal:  PLoS One       Date:  2014-05-30       Impact factor: 3.240

9.  Two brothers with reduced vision.

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Journal:  Oman J Ophthalmol       Date:  2017 Sep-Dec

10.  Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

Authors:  Adriana I Iglesias; Aniket Mishra; Veronique Vitart; Yelena Bykhovskaya; René Höhn; Henriët Springelkamp; Gabriel Cuellar-Partida; Puya Gharahkhani; Jessica N Cooke Bailey; Colin E Willoughby; Xiaohui Li; Seyhan Yazar; Abhishek Nag; Anthony P Khawaja; Ozren Polašek; David Siscovick; Paul Mitchell; Yih Chung Tham; Jonathan L Haines; Lisa S Kearns; Caroline Hayward; Yuan Shi; Elisabeth M van Leeuwen; Kent D Taylor; Pieter Bonnemaijer; Jerome I Rotter; Nicholas G Martin; Tanja Zeller; Richard A Mills; Emmanuelle Souzeau; Sandra E Staffieri; Jost B Jonas; Irene Schmidtmann; Thibaud Boutin; Jae H Kang; Sionne E M Lucas; Tien Yin Wong; Manfred E Beutel; James F Wilson; André G Uitterlinden; Eranga N Vithana; Paul J Foster; Pirro G Hysi; Alex W Hewitt; Chiea Chuen Khor; Louis R Pasquale; Grant W Montgomery; Caroline C W Klaver; Tin Aung; Norbert Pfeiffer; David A Mackey; Christopher J Hammond; Ching-Yu Cheng; Jamie E Craig; Yaron S Rabinowitz; Janey L Wiggs; Kathryn P Burdon; Cornelia M van Duijn; Stuart MacGregor
Journal:  Nat Commun       Date:  2018-05-14       Impact factor: 14.919

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